A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858928



Internal ID22633863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5978128..5979145hg38UCSC Ensembl
chr9:5978128..5979145hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381018
hg191018
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513755
Samples
Known GenesKIAA2026
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858928
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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